1,604 research outputs found

    Protective effects of urocortin 2 against caerulein-induced acute pancreatitis.

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    Because little is known about the role of corticotropin-releasing factor (CRF) agonists in regulating responses in pancreatitis, we evaluated the effects of urocortin 2 (UCN2) and stressin1 in caerulein-induced acute pancreatitis (AP) model in rats. Male rats were pretreated with UCN2 or stressin1 for 30 min followed by induction of AP with supraphysiologic doses of caerulein. Serum amylase and lipase activity, pancreatic tissue necrosis, immune cell infiltrate, nuclear factor (NF)-κB activity, trypsin levels, and intracellular Ca2+ ([Ca2+]i) were ascertained. UCN2, but not stressin1 attenuated the severity of AP in rats. UCN2, but not stressin1, reduced serum amylase and lipase activity, cell necrosis and inflammatory cell infiltration in AP. NF-κB activity in pancreatic nuclear extracts increased in AP and UCN2 treatment reduced caerulein-induced increases in NF-κB activity by 42%. UCN2 treatment prevented caerulein-induced degradation of IκB-α in the cytosolic fraction as well as increased levels of p65 subunit of NF-κB in the cytosolic fraction. Pancreatic UCN2 levels decreased in AP compared with saline. UCN2 evoked [Ca2+]i responses in primary acinar cells and abolished caerulein-evoked [Ca2+]i responses at 0.1nM, and decreased by ~50% at 1.0nM caerulein. UCN2 stimulation resulted in redistribution of a portion of F-actin from the apical to the basolateral pole. UCN2 prevented the massive redistribution of F-actin observed with supraphysiologic doses of caerulein. UCN2, but not stressin1 attenuated severity of an experimental pancreatitis model. The protective effects of UCN2, including anti-inflammatory and anti-necrotic effects involve activation of the CRF2 receptor, [Ca2+]i signaling, and inhibition of NF-κB activity

    The perimeter of large planar Voronoi cells: a double-stranded random walk

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    Let p_np\_n be the probability for a planar Poisson-Voronoi cell to have exactly nn sides. We construct the asymptotic expansion of logp_n\log p\_n up to terms that vanish as nn\to\infty. We show that {\it two independent biased random walks} executed by the polar angle determine the trajectory of the cell perimeter. We find the limit distribution of (i) the angle between two successive vertex vectors, and (ii) the one between two successive perimeter segments. We obtain the probability law for the perimeter's long wavelength deviations from circularity. We prove Lewis' law and show that it has coefficient 1/4.Comment: Slightly extended version; journal reference adde

    Asymptotic statistics of the n-sided planar Poisson-Voronoi cell. I. Exact results

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    We achieve a detailed understanding of the nn-sided planar Poisson-Voronoi cell in the limit of large nn. Let p_n{p}\_n be the probability for a cell to have nn sides. We construct the asymptotic expansion of logp_n\log {p}\_n up to terms that vanish as nn\to\infty. We obtain the statistics of the lengths of the perimeter segments and of the angles between adjoining segments: to leading order as nn\to\infty, and after appropriate scaling, these become independent random variables whose laws we determine; and to next order in 1/n1/n they have nontrivial long range correlations whose expressions we provide. The nn-sided cell tends towards a circle of radius (n/4\pi\lambda)^{\half}, where λ\lambda is the cell density; hence Lewis' law for the average area A_nA\_n of the nn-sided cell behaves as A_ncn/λA\_n \simeq cn/\lambda with c=1/4c=1/4. For nn\to\infty the cell perimeter, expressed as a function R(ϕ)R(\phi) of the polar angle ϕ\phi, satisfies d2R/dϕ2=F(ϕ)d^2 R/d\phi^2 = F(\phi), where FF is known Gaussian noise; we deduce from it the probability law for the perimeter's long wavelength deviations from circularity. Many other quantities related to the asymptotic cell shape become accessible to calculation.Comment: 54 pages, 3 figure

    The effect of 'Astressin', a novel antagonist of corticotropin releasing hormone (CRH), on CRH-induced seizures in the infant rat: comparison with two other antagonists.

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    Corticotropin releasing hormone (CRH) has both neuroendocrine effects, promoting ACTH release from the anterior pituitary, and neurotransmitter properties, acting on specific neuronal populations. A recently designed CRH analogue has been shown to be highly potent in preventing activation of pituitary CRH receptors. The efficacy of this compound, 'Astressin', in blocking the effects of CRH in the central nervous system (CNS) has not been determined. CRH induces prolonged amygdala-origin seizures in neonatal and infant rats. This model was used in the current study, to compare Astressin to alpha-helical CRH-(9-41), and to [D-Phe12, Nle21.38, C-MeLeu37]CRH-(12-41), i.e. D-Phe-CRH-(12-41). Astressin (3 or 10 micrograms) was infused into the cerebral ventricles of infant rats prior to CRH infusion. Both doses of the analogue significantly delayed the onset of CRH-induced seizures when given 15, but not 30 min before CRH. No effect of the lower Astressin dose on seizure duration was demonstrated; the higher dose prevented seizures in 2/12 rats, and delayed seizure onset in the others (22.7 +/- 5 min vs 10.1 +/- 1.3 min). In the same paradigm, 10 micrograms of alpha-helical CRH-(9-41) and 5 micrograms of D-Phe-CRH-(12-41) had comparable effects on seizure latency and duration. Electroencephalograms confirmed the behavioral effects of Astressin. Therefore, in a CNS model of CRH-mediated neurotransmission, the potency of Astressin is not substantially higher than that of alpha-helical CRH (9-41) and D-Phe-CRH-(12-41)

    On Random Bubble Lattices

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    We study random bubble lattices which can be produced by processes such as first order phase transitions, and derive characteristics that are important for understanding the percolation of distinct varieties of bubbles. The results are relevant to the formation of topological defects as they show that infinite domain walls and strings will be produced during appropriate first order transitions, and that the most suitable regular lattice to study defect formation in three dimensions is a face centered cubic lattice. Another application of our work is to the distribution of voids in the large-scale structure of the universe. We argue that the present universe is more akin to a system undergoing a first-order phase transition than to one that is crystallizing, as is implicit in the Voronoi foam description. Based on the picture of a bubbly universe, we predict a mean coordination number for the voids of 13.4. The mean coordination number may also be used as a tool to distinguish between different scenarios for structure formation.Comment: several modifications including new abstract, comparison with froth models, asymptotics of coordination number distribution, further discussion of biased defects, and relevance to large-scale structur

    From one cell to the whole froth: a dynamical map

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    We investigate two and three-dimensional shell-structured-inflatable froths, which can be constructed by a recursion procedure adding successive layers of cells around a germ cell. We prove that any froth can be reduced into a system of concentric shells. There is only a restricted set of local configurations for which the recursive inflation transformation is not applicable. These configurations are inclusions between successive layers and can be treated as vertices and edges decorations of a shell-structure-inflatable skeleton. The recursion procedure is described by a logistic map, which provides a natural classification into Euclidean, hyperbolic and elliptic froths. Froths tiling manifolds with different curvature can be classified simply by distinguishing between those with a bounded or unbounded number of elements per shell, without any a-priori knowledge on their curvature. A new result, associated with maximal orientational entropy, is obtained on topological properties of natural cellular systems. The topological characteristics of all experimentally known tetrahedrally close-packed structures are retrieved.Comment: 20 Pages Tex, 11 Postscript figures, 1 Postscript tabl

    Asymptotic statistics of the n-sided planar Voronoi cell: II. Heuristics

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    We develop a set of heuristic arguments to explain several results on planar Poisson-Voronoi tessellations that were derived earlier at the cost of considerable mathematical effort. The results concern Voronoi cells having a large number n of sides. The arguments start from an entropy balance applied to the arrangement of n neighbors around a central cell. It is followed by a simplified evaluation of the phase space integral for the probability p_n that an arbitrary cell be n-sided. The limitations of the arguments are indicated. As a new application we calculate the expected number of Gabriel (or full) neighbors of an n-sided cell in the large-n limit.Comment: 22 pages, 10 figure

    Topological correlations in soap froths

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    Correlation in two-dimensional soap froth is analysed with an effective potential for the first time. Cells with equal number of sides repel (with linear correlation) while cells with different number of sides attract (with NON-bilinear) for nearest neighbours, which cannot be explained by the maximum entropy argument. Also, the analysis indicates that froth is correlated up to the third shell neighbours at least, contradicting the conventional ideas that froth is not strongly correlated.Comment: 10 Pages LaTeX, 6 Postscript figure

    LES NOYAUX DE TRANSITION 189Ir ET 187Ir SONT-ILS TRIAXIAUX ?

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    Les niveaux excités des noyaux 189Ir et 187Ir ont été étudiés par réaction (α, 2nγ) sur le faisceau du cyclotron de Grenoble. Les schémas détaillés qui ont été établis mettent en évidence : 1) des états de parité positive qui s'interprètent comme appartenant aux deux bandes 3/2+ | 402 | (fondamental) et 1/2+ | 400 | mélangées par interaction de Coriolis (noyaux a symétrie axiale de déformation positive) ; 2) une bande découplée construite sur un état 9/2- (h 9/2) décrite de manière équivalente par un modèle à symétrie axiale et déformation positive ou par un modèle a particule-plus-rotor asymétrique ; 3) une structure complexe pour les niveaux de parité négative associés à l'isomère 11/2- (h 11/2). Ce système est correctement prédit par le modèle à rotor asymétrique
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